CN101389684B - Curable epoxy resin composition - Google Patents
Curable epoxy resin composition Download PDFInfo
- Publication number
- CN101389684B CN101389684B CN2007800064020A CN200780006402A CN101389684B CN 101389684 B CN101389684 B CN 101389684B CN 2007800064020 A CN2007800064020 A CN 2007800064020A CN 200780006402 A CN200780006402 A CN 200780006402A CN 101389684 B CN101389684 B CN 101389684B
- Authority
- CN
- China
- Prior art keywords
- expression
- compound
- group
- epoxy
- substituting group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 0 CC1=CCCC=C1* Chemical compound CC1=CCCC=C1* 0.000 description 3
- FHHMKBZHLJHCMX-UHFFFAOYSA-N C(C1OC1)Oc1cccc(Oc2cccc(-c3nc(ccc(-c(cc4)cc5c4nc(-c4cc(Oc6cccc(OCC7OC7)c6)ccc4)[o]5)c4)c4[o]3)c2)c1 Chemical compound C(C1OC1)Oc1cccc(Oc2cccc(-c3nc(ccc(-c(cc4)cc5c4nc(-c4cc(Oc6cccc(OCC7OC7)c6)ccc4)[o]5)c4)c4[o]3)c2)c1 FHHMKBZHLJHCMX-UHFFFAOYSA-N 0.000 description 2
- OECWSZHBHKUFNQ-UHFFFAOYSA-N C(C1OC1)Oc(cc1)ccc1-c1nc(ccc(-c(cc2)cc3c2nc(-c(cc2)ccc2OCC2OC2)[o]3)c2)c2[o]1 Chemical compound C(C1OC1)Oc(cc1)ccc1-c1nc(ccc(-c(cc2)cc3c2nc(-c(cc2)ccc2OCC2OC2)[o]3)c2)c2[o]1 OECWSZHBHKUFNQ-UHFFFAOYSA-N 0.000 description 1
- FKBMTBAXDISZGN-UHFFFAOYSA-N CC(CCC1C(O2)=O)CC1C2=O Chemical compound CC(CCC1C(O2)=O)CC1C2=O FKBMTBAXDISZGN-UHFFFAOYSA-N 0.000 description 1
- MYYWOKTUWMVNOO-UHFFFAOYSA-N O=C(c(cc1)ccc1OCC1OC1)Nc1ccc2[o]c(-c(cc3)ccc3OCC3OC3)nc2c1 Chemical compound O=C(c(cc1)ccc1OCC1OC1)Nc1ccc2[o]c(-c(cc3)ccc3OCC3OC3)nc2c1 MYYWOKTUWMVNOO-UHFFFAOYSA-N 0.000 description 1
- LPHDMFIPBJDCCQ-UHFFFAOYSA-N Oc(cc1)ccc1-c1nc(ccc(-c(cc2)cc3c2nc(-c(cc2)ccc2O)[o]3)c2)c2[o]1 Chemical compound Oc(cc1)ccc1-c1nc(ccc(-c(cc2)cc3c2nc(-c(cc2)ccc2O)[o]3)c2)c2[o]1 LPHDMFIPBJDCCQ-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
- C08G59/22—Di-epoxy compounds
- C08G59/26—Di-epoxy compounds heterocyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/18—Benzimidazoles; Hydrogenated benzimidazoles with aryl radicals directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/56—Benzoxazoles; Hydrogenated benzoxazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/56—Benzoxazoles; Hydrogenated benzoxazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D263/57—Aryl or substituted aryl radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/4007—Curing agents not provided for by the groups C08G59/42 - C08G59/66
- C08G59/4014—Nitrogen containing compounds
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/03—Use of materials for the substrate
- H05K1/0313—Organic insulating material
- H05K1/032—Organic insulating material consisting of one material
- H05K1/0326—Organic insulating material consisting of one material containing O
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Epoxy Resins (AREA)
Abstract
An epoxy resin curing composition is characterized by containing a compound having a benzoxazole structure represented by formula (I): wherein X<1> and X<2>, which may be the same or different, each represents hydrogen, a substituent having a phenolic hydroxyl group, or a substituent having an epoxy group, provided that X<1> and X<2> are not hydrogen atoms at the same time; or X<1> and X<2> are taken together to form a 3- to 8-membered, saturated or unsaturated heterocyclic ring substituted with a substituent having a phenolic hydroxyl group or a substituent having an epoxy group; Y1 represents oxygen or sulfur; Z<1> represents a substituted or unsubstituted C1-C8 hydrocarbon group or a substituted or unsubstituted C1-C8 alkoxy group; m is an integer of 0 to 4; when m is 2 to 4, a plurality of Z<1>s may be the same or different; n is an integer of 0 to 2; and A<1> represents hydrogen, a substituent having a phenolic hydroxyl group or a substituent having an epoxy group.
Description
Technical field
The present invention relates to comprise the phenolic compound of
the azoles structure that has benzo or have the curable epoxy resin composition of the epoxy compounds of benzo
azoles structure; In more detail; The present invention relates to phenolic compound as curing agent for epoxy resin or to have the curable epoxy resin composition that epoxy compounds is little as epoxy resin and linear expansivity, tensile strength is excellent of benzo
azoles structure, further to relate to the novel cpd of
the azoles structure that has benzo with benzo
azoles structure.
Background technology
In the tellite, consider that the epoxy resin that is widely used in recent years, in the densification process that is accompanied by the miniaturized lighting, is also studied in the processing to epoxy resin from its characteristic.
Particularly remain in high second-order transition temperature, volume specific resistance, mechanical characteristics and the low water-absorbent that the bonding strength between thin layerization, conductor layer and the insulation layer that plating resist on the tellite requires to have the heating that distribution was caused that can tackle Highgrade integration and insulation layer descends as insulation layer with the mode of lamination (build-up).
In addition, the epoxy resin that is used for preimpregnation material etc. reduces polar expansion through mixing various mineral fillers, suppresses because the distortion that temperature causes.But, if mix mineral filler, drawback being arranged then, tensile strength and elongation reduce, or owing to aggegation causes short circuit, the safety of infringement circuit etc.
As epoxy resin, the widely known universal product is the diglycidylether of dihydroxyphenyl propane, is well known that widely that also polyphenolic substance such as phenol phenolic varnish can be used as curing agent for epoxy resin and uses.
In non-patent literature 1, put down in writing various phenols curing agents, also put down in writing with have addition on the heteroatomic condensed ring compound of structure of phenol as curing agent for epoxy resin, form p-hydroxybenzene maleimide/butyl acrylate copolymer.
Record is with the polyamide resin that contains phenol property hydroxyl and the epoxy resin composition epoxy resin as constituent in patent documentation 1～3.
But these existing composition epoxy resins can't obtain enough performances aspect rerum naturas such as linear expansivity and tensile strength, elongation.
In addition; In patent documentation 4, put down in writing the phenolic compound of
the azoles structure that has benzo; But this phenolic compound can't use as the solidifying agent of epoxy compounds, and the polymkeric substance that obtains neither epoxy resin.
Patent documentation 1: the spy opens the 2001-31784 communique
Patent documentation 2: the spy opens the 2001-49082 communique
Patent documentation 3: the spy opens the 2005-29720 communique
Patent documentation 4: No. 5270432 specification sheets of USP
Non-patent literature 1: " new development of epoxy curing agent ", P154, CMC Co., Ltd., on May 31st, 1994
Summary of the invention
Even providing, the present invention do not use filler, the curable epoxy resin composition that rerum naturas such as linear expansivity is low, tensile strength and elongation are also excellent.
The inventor etc. have carried out conscientiously research according to above-mentioned present situation; The result find through with phenolic compound with benzo
azoles structure as curing agent for epoxy resin, or with epoxy compounds with benzo
azoles structure as epoxy resin; Can obtain that linear expansivity is low, the curable epoxy resin composition of physical properties excellent such as tensile strength and elongation, thereby accomplished the present invention.
Promptly; The present invention realizes above-mentioned purpose through a kind of curable epoxy resin composition is provided, and this curable epoxy resin composition is characterised in that: the compound with benzo
azoles structure that contains formula (I) expression.
[in the formula, X
1And X
2Substituting group (but the X that separately independently of each other, can represent Wasserstoffatoms identical or differently, have the substituting group of phenol property hydroxyl or have epoxy group(ing)
1And X
2Be not Wasserstoffatoms simultaneously), perhaps, X
1And X
2Can be cross-linked with each other and form atomicity is 3～8 saturated or undersaturated heterocycle, and the substituting group that aforementioned saturated or undersaturated heterocycle comprises the substituting group with phenol property hydroxyl or has an epoxy group(ing) is as substituting group.Y
1Expression Sauerstoffatom or sulphur atom.Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different.N representes 0～2 integer.A
1Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).]
In addition, the present invention realizes above-mentioned purpose through above-mentioned curable epoxy resin composition is provided, and this curable epoxy resin composition is characterised in that: in the above-mentioned general formula (I), and X
1Or X
2In any represent with formula (Ia).
[in the formula, Y
1Expression Sauerstoffatom or sulphur atom, Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different.N representes 0～2 integer.A
1Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).]
In addition, the present invention realizes above-mentioned purpose through a kind of curable epoxy resin composition is provided, and this curable epoxy resin composition is characterised in that: in the above-mentioned general formula (I), and X
1Or X
2In any represent with formula (Ib).
[in the formula, Y
1Expression Sauerstoffatom or sulphur atom, Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different.N representes 0～2 integer.A
1Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).]
In addition, the present invention realizes above-mentioned purpose through a kind of curable epoxy resin composition is provided, and this curable epoxy resin composition is characterised in that: in the above-mentioned general formula (I), and X
1And X
2The heterocycle that is cross-linked with each other and forms formula (Ic) or (Id) represent.
[in the formula, Y
1Expression Sauerstoffatom or sulphur atom, Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different.A
1Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).]
[in the formula, Y
1Expression Sauerstoffatom or sulphur atom, Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different.A
1Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).]
In addition, the present invention realizes above-mentioned purpose through a kind of curable epoxy resin composition is provided, and this curable epoxy resin composition is characterised in that: in the above-mentioned general formula (I), and A
1It is substituting group with epoxy group(ing).
In addition; The present invention realizes above-mentioned purpose through a kind of curable epoxy resin composition is provided, and this curable epoxy resin composition is characterised in that: the compound with benzo
azoles structure that contains formula (II) expression.
[in the formula, Y
2Expression Sauerstoffatom or sulphur atom.Z
2Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, r representes 0～3 integer, r is 2～3 o'clock, a plurality of Z
2Can be the same or different.P representes 0～2 integer.Q representes 1～100 number.A
2Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).]
In addition; The present invention realizes above-mentioned purpose through a kind of curable epoxy resin composition is provided, and this curable epoxy resin composition is characterised in that: the compound with benzo
azoles structure that contains formula (III) expression.
[in the formula, Y
3Expression Sauerstoffatom or sulphur atom.Z
3Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, t representes 0～3 integer, t is 2～3 o'clock, a plurality of Z
3Can be the same or different.S representes 1～100 number.A
3Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).]
In addition; The present invention realizes above-mentioned purpose through a kind of curable epoxy resin composition is provided, and this curable epoxy resin composition is characterised in that: the compound with benzo
azoles structure that contains formula (IV) expression.
[in the formula, Y
4Expression Sauerstoffatom or sulphur atom.Z
4Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, v representes 0～3 integer, v is 2～3 o'clock, a plurality of Z
4Can be the same or different.U representes 1～100 number.A
4Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).]
In addition, the present invention realizes above-mentioned purpose through a kind of curable epoxy resin composition is provided, and this curable epoxy resin composition is characterised in that: the A in the above-mentioned general formula (II)
2, the A in the above-mentioned general formula (III)
3Or the A in the above-mentioned general formula (IV)
4It is substituting group with epoxy group(ing).
In addition, also through providing a kind of veneer sheet to realize above-mentioned purpose with solidification compound, this veneer sheet has used above-mentioned curable epoxy resin composition with solidification compound in the present invention.
In addition, also through providing a kind of cured article to realize above-mentioned purpose, this cured article obtains through above-mentioned curable epoxy resin composition is solidified in the present invention.
In addition, the present invention realizes above-mentioned purpose through a kind of novel benzo
azole compounds with formula (V) expression is provided.
[in the formula, Y
1Expression Sauerstoffatom or sulphur atom.Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different.N representes 0～2 integer.A
1The substituting group that expression has the substituting group of phenol property hydroxyl or has epoxy group(ing).]
In addition, the present invention realizes above-mentioned purpose through a kind of novel benzo
azole compounds with formula (VI) expression is provided.
[in the formula, Y
1Expression Sauerstoffatom or sulphur atom, Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different.N representes 0～2 integer.A
1The substituting group that expression has the substituting group of phenol property hydroxyl or has epoxy group(ing).]
Description of drawings
Fig. 1 is the figure of the lamination of expression vacuum pressing (vacuum pressing) method.
Fig. 2 is a compound N IR spectrogram o.12.
Fig. 3 is a compound N IR spectrogram o.13.
Fig. 4 is a compound N IR spectrogram o.4.
Fig. 5 is a compound N IR spectrogram o.14.
Embodiment
Below, embodiment preferred of the present invention is elaborated.
Curable epoxy resin composition of the present invention contains the compound with benzo
azoles structure of formula (I) expression.
[in the formula, X
1And X
2Substituting group (still, the X that separately independently of each other, can represent Wasserstoffatoms identical or differently, have the substituting group of phenol property hydroxyl or have epoxy group(ing)
1And X
2Be not Wasserstoffatoms simultaneously), perhaps, X
1And X
2Can be cross-linked with each other and form atomicity is 3～8 saturated or undersaturated heterocycle, and the substituting group that aforementioned saturated or undersaturated heterocycle comprises the substituting group with phenol property hydroxyl or has an epoxy group(ing) is as substituting group.Y
1Expression Sauerstoffatom or sulphur atom.Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different.N representes 0～2 integer.A
1Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).]
In the above-mentioned general formula (I), described have the substituting group of phenol property hydroxyl so long as in substituting group, have the group of phenol property hydroxyl and get final product, and can certainly be phenylol.As an example, can enumerate out the substituting group of formula (VII) expression.
[in the formula, B
1The expression substituting group, w representes 0～4 number.Substituent B
1Do not have special qualification, can enumerate out organic groups such as alkyl, alkoxyl group, aryl, w is 2～4 o'clock, a plurality of B
1Can be the same or different].
From the rerum natura aspect of cured articles such as manufacturing cost and the expansion of hot line property, above-mentioned phenylol with preferred w=0 of substituting group of phenol property hydroxyl.
In addition, in the above-mentioned general formula (I), described have the substituting group of epoxy group(ing) so long as in substituting group, have the group of epoxy group(ing) and get final product, and also can have other substituting group.As an example, can enumerate out the substituting group that epoxy group(ing), ester ring type epoxy group(ing), glycidyl perhaps have the glycidyl of formula (VIII) expression.
[in the formula, Ar representes can have substituent alkylidene group, can have substituent arylidene, and this alkylidene group and arylidene can be interrupted by unsaturated link(age), ehter bond, thioether bond, ester bond.]
Example as above-mentioned alkylidene group or arylidene; Can enumerate out methylene radical, ethylidene, propylidene, butylidene, phenylene etc.; From the rerum natura aspect of manufacturing cost with cured articles such as reactivity, hotline expansion coefficient, second-order transition temperature points, preferred alkylidene group or phenylene.
From manufacturing cost and rerum natura aspect, above-mentioned substituting group with epoxy group(ing) is glycidyl or have the substituting group of the glycidyl of above-mentioned general formula (VIII) expression preferably.
In general formula (I), Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different, but from manufacturing cost and rerum natura aspect, m is preferably 0.
In addition, can to have substituent carbonatoms be 1～8 alkyl as above-mentioned, can enumerate out alkyl such as methyl, ethyl, sec.-propyl, naphthenic base such as cyclohexyl, aryl such as phenyl etc.; As this substituting group, can enumerate out alkoxyl groups such as halogen atom, trifluoromethyl, methoxyl group, hydroxyl etc.In addition, can to have substituent carbonatoms be 1～8 alkoxyl group as above-mentioned, can enumerate out phenyl ether, alkylether radicals, phenoxy, methoxyl group etc.; As this substituting group, can enumerate out halogen atom, trifluoromethyl, hydroxyl, methoxyl group etc.
X
1And X
2Can be cross-linked with each other and form atomicity is 3～8 saturated or undersaturated heterocycle, and the substituting group that aforementioned saturated or undersaturated heterocycle can comprise the substituting group with phenol property hydroxyl or have an epoxy group(ing) is as substituting group.
When the formation atomicity is 3～8 saturated or undersaturated heterocycle; As this saturated heterocycle; Can enumerate out morpholine etc.; As this unsaturated heterocycle, can enumerate out
azoles, thiazole etc.
The benzo that has in above-mentioned general formula (I) expression
In the compound of azoles structure, from the rerum natura aspect of manufacturing cost, as preferably having benzo with cured articles such as reactivity, linear expansivity, second-order transition temperature points
The compound of azoles structure can be enumerated out: X
1Or X
2In any benzo that has with formula (Ia) expression
The compound of azoles structure.
[in the formula, Y
1Expression Sauerstoffatom or sulphur atom, Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different.N representes 0～2 integer.A
1Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).]
In above-mentioned general formula (Ia), have phenol property hydroxyl substituting group, have an epoxy group(ing) substituting group and aforementioned formula (I) in put down in writing identical, preferably those are also identical.In addition, m also and general formula (I) be preferably 0 equally.
In addition, at the benzo that has of general formula (I) expression
In the compound of azoles structure, from the rerum natura aspect of manufacturing cost, as preferably having benzo with cured articles such as reactivity, hotline expansion coefficient, second-order transition temperature points
The compound of azoles structure can be enumerated out: X
1Or X
2In any benzo that has with formula (Ib) expression
The compound of azoles structure.
[in the formula, Y
1Expression Sauerstoffatom or sulphur atom, Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different.A
1Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).]
In above-mentioned general formula (Ib), have phenol property hydroxyl substituting group, have an epoxy group(ing) substituting group and aforementioned formula (I) in put down in writing identical, preferably those are also identical.In addition, m also and general formula (I) be preferably 0 equally.
In addition, at the benzo that has of general formula (I) expression
In the compound of azoles structure, from the rerum natura aspect of manufacturing cost, as preferably having benzo with cured articles such as reactivity, hotline expansion coefficient, second-order transition temperature points
The compound of azoles structure can be enumerated out: X
1Or X
2Be cross-linked with each other form with formula (Ic) or (Id) heterocyclic of expression have benzo
The compound of azoles structure.
[in the formula, Y
1Expression Sauerstoffatom or sulphur atom, Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different.A
1Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).]
At above-mentioned general formula (Ic) or (Id), have phenol property hydroxyl substituting group, have an epoxy group(ing) substituting group and aforementioned formula (I) in put down in writing identical, preferably those are also identical.In addition, m also and general formula (I) be preferably 0 equally.
The benzo that has in above-mentioned general formula (I) expression
In the compound of azoles structure, X
1And X
2Be cross-linked with each other and form atomicity when being 3～8 saturated or undersaturated heterocycle, from the rerum natura aspect of cured articles such as manufacturing cost, reactivity, hotline expansion coefficient, second-order transition temperature point, preferred atomicity is 5 unsaturated heterocycle.
Described general formula (I) expression have a benzo
The compound of azoles structure has the situation of phenol property hydroxyl, is meant A
1Be the situation of substituting group (also comprising phenylol itself) and the situation of Wasserstoffatoms with phenol property hydroxyl; Described situation with epoxy group(ing) is meant A
1It is the situation of substituting group (also comprising epoxy group(ing) itself) with epoxy group(ing).
The compound with benzo
azoles structure of general formula of the present invention (I) expression is when having phenol property hydroxyl; This compound preferably uses as curing agent for epoxy resin (being also referred to as phenols curing agent); In curable epoxy resin composition; The content of this compound especially is preferably 10 quality %～90 quality %, more preferably 30 quality %～80 quality %.
The compound with benzo
azoles structure of general formula of the present invention (I) expression is when having epoxy group(ing); Preferably use as epoxy composition (being also referred to as epoxy resin); In curable epoxy resin composition; The content of this compound especially is preferably 10 quality %～90 quality %, more preferably 30 quality %～80 quality %.
Then, the compound of mutual-through type (II) describes.Curable epoxy resin composition of the present invention comprises the compound with benzo
azoles structure of formula (II) expression.
[in the formula, Y
2Expression Sauerstoffatom or sulphur atom.Z
2Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, r representes 0～3 integer, r is 2～3 o'clock, a plurality of Z
2Can be the same or different.P representes 0～2 integer.Q representes 1～100 number.A
2Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).]
In above-mentioned general formula (II), have phenol property hydroxyl substituting group, have an epoxy group(ing) substituting group and aforementioned formula (I) in put down in writing identical, preferably those are also identical.In addition, r is preferably 0 from manufacturing cost and rerum natura aspect.Q is preferably 1～10 from manufacturing cost, dissolution with solvents degree, resin affinity and reactive aspect.
General formula (II) expression have a benzo
The compound of azoles structure has the situation of phenol property hydroxyl, is meant A
2Be the situation of substituting group (also comprising phenylol itself) and the situation of Wasserstoffatoms with phenol property hydroxyl; Have the situation of epoxy group(ing), be meant A
2It is the situation of substituting group (also comprising epoxy group(ing) itself) with epoxy group(ing).
The compound with benzo
azoles structure of general formula of the present invention (II) expression has under the situation of phenol property hydroxyl; This compound preferably uses as curing agent for epoxy resin (being also referred to as phenols curing agent); In curable epoxy resin composition; The content of this compound especially is preferably 10 quality %～90 quality %, more preferably 30 quality %～80 quality %.
The compound with benzo
azoles structure of general formula of the present invention (II) expression has under the situation of epoxy group(ing); This compound preferably uses as epoxy composition (being also referred to as epoxy resin); In curable epoxy resin composition; The content of this compound especially is preferably 10 quality %～90 quality %, more preferably 30 quality %～80 quality %.
Then, the compound of mutual-through type (III) describes.Curable epoxy resin composition of the present invention comprises the compound with benzo
azoles structure of formula (III) expression.
[in the formula, Y
3Expression Sauerstoffatom or sulphur atom.Z
3Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, t representes 0～3 integer, t is 2～3 o'clock, a plurality of Z
3Can be the same or different.S representes 1～100 number.A
3Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).]
In above-mentioned general formula (III), have phenol property hydroxyl substituting group, have an epoxy group(ing) substituting group and aforementioned formula (I) in put down in writing identical, preferably those are also identical.In addition, from manufacturing cost and rerum natura aspect, t is preferably 0.From manufacturing cost, dissolution with solvents degree, resin affinity and reactive aspect, s is preferably 1～10.
Described general formula (III) expression have a benzo
The compound of azoles structure has the situation of phenol property hydroxyl, is meant A
3Be the situation of substituting group (also comprising phenylol itself) and the situation of Wasserstoffatoms with phenol property hydroxyl; Have the situation of epoxy group(ing), be meant A
3It is the situation of substituting group (also comprising epoxy group(ing) itself) with epoxy group(ing).
The compound with benzo
azoles structure of general formula (III) expression has under the situation of phenol property hydroxyl; This compound preferably uses as curing agent for epoxy resin (being also referred to as phenols curing agent); In curable epoxy resin composition; The content of this compound especially is preferably 10 quality %～90 quality %, more preferably 30 quality %～80 quality %.
The compound with benzo
azoles structure of general formula (III) expression has under the situation of epoxy group(ing); It preferably uses as epoxy composition (being also referred to as epoxy resin); In curable epoxy resin composition; The content of this compound especially is preferably 10 quality %～90 quality %, more preferably 30 quality %～80 quality %.
Then, the compound of mutual-through type (IV) describes.Curable epoxy resin composition of the present invention comprises the compound with benzo
azoles structure of formula (IV) expression.
[in the formula, Y
4Expression Sauerstoffatom or sulphur atom.Z
4Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, v representes 0～3 integer, v is 2～3 o'clock, a plurality of Z
4Can be the same or different.U representes 1～100 number.A
4Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).]
In above-mentioned general formula (IV), have phenol property hydroxyl substituting group, have an epoxy group(ing) substituting group and aforementioned formula (I) in put down in writing identical, preferably those are also identical.In addition, from manufacturing cost and rerum natura aspect, v is preferably 0.From manufacturing cost, dissolution with solvents degree, resin affinity and reactive aspect, u is preferably 1～10.
General formula (IV) expression have a benzo
The compound of azoles structure has the situation of phenol property hydroxyl, is meant A
4Be the situation of substituting group (also comprising phenylol itself) and the situation of Wasserstoffatoms with phenol property hydroxyl; Have the situation of epoxy group(ing), be meant A
4It is the situation of substituting group (also comprising epoxy group(ing) itself) with epoxy group(ing).
The compound with benzo
azoles structure of general formula (IV) expression has under the situation of phenol property hydroxyl; This compound preferably uses as curing agent for epoxy resin (being also referred to as phenols curing agent); In curable epoxy resin composition; The content of this compound especially is preferably 10 quality %～90 quality %, more preferably 30 quality %～80 quality %.
The compound with benzo
azoles structure of general formula (IV) expression is when having epoxy group(ing); Preferably use as epoxy composition (being also referred to as epoxy resin); In curable epoxy resin composition; The content of this compound especially is preferably 10 quality %～90 quality %, more preferably 30 quality %～80 quality %.
More specifically explain for compound with benzo
azoles structure and situation with phenol property hydroxyl.
As the structure more specifically of the compound with phenol property hydroxyl of general formula (I) expression, the structure of No.1～8 below for example can enumerating out; As the concrete structure of the compound with phenol property hydroxyl of general formula (II) expression, can enumerate out the structure of following No.9; Likewise,, the compound of No.10-1 can be enumerated out,, the compound of No.10-2 can be enumerated out as the compound of general formula (IV) as the compound of general formula (III) expression.But the present invention does not receive any restriction of following structure.
Compound method as the compound with phenol property hydroxyl (being also referred to as phenolic compound) of general formula (I) expression; Can become through carrying out
piperazine cyclization with benzoic acid derivative from the dihydroxybiphenyl sulfonamide derivatives, in compound, obtain benzo
azoles structure thus.If o.2 with above-mentioned compound N is that example is elaborated; At first as following reaction formula (A), carry out
piperazine cyclization.Promptly; Make 3; 3-dihydroxybiphenyl amine and 4-fluorinated acid carry out benzo
piperazine reaction in solvent; Obtain fluorochemical (2,2 '-two (4-fluoro phenyl) dibenzo
azoles).Then, as following reaction formula (B), in solvent, alkali in the presence of, make fluorochemical and resorcin reaction, carry out etherification reaction again, can obtain the phenolic compound of above-claimed cpd No.3.
Reaction formula (A)
Reaction formula (B)
Then; Compound method as the compound with phenol property hydroxyl (being also referred to as phenolic compound) of general formula (II) expression; So long as after using triphenyl phosphite-pyridines condensing agent to make the diaminobenzene amphyl carry out the direct condensation reaction, heat, carry out ring-closure reaction and get final product with the hydroxyl phthalic verivate.The direct condensation reaction of use triphenyl phosphite-pyridines condensing agent can be with reference to Japanization association volume, " the 4th edition experimental chemistry lecture 28 Polymer Synthesizings " the 266th page (ball be apt to Co., Ltd., puts down into distribution on May 6th, 4).If o.9 with above-mentioned compound N is that example is elaborated, be with amidol and 5-hydroxyl m-phthalic acid in the N-Methyl pyrrolidone solvent, in the presence of triphenyl phosphite, pyridine, lithium chloride, carry out polycondensation.After the reaction, take out polycondensate, carry out ring-closure reaction through heat treated and get final product.
Then; As the general formula (III) or (IV) compound method of the compound with phenol property hydroxyl (being also referred to as phenolic compound) of expression; So long as likewise use triphenyl phosphite-pyridines condensing agent to make diamino resorcin verivate and hydroxyl phthalic verivate carry out heating, carrying out ring-closure reaction and get final product after direct condensation reacts with the compound method of the compound with phenol property hydroxyl of above-mentioned general formula (II) expression.If o.10-1 with above-mentioned compound N is that example is elaborated; Be with 4; 6-diamino resorcin dihydrochloride and 5-hydroxyl m-phthalic acid in the presence of triphenyl phosphite, pyridine, lithium chloride, carry out polycondensation in the N-Methyl pyrrolidone solvent.After the reaction, take out polycondensate, carry out ring-closure reaction through heat treated and get final product.
Compound with benzo
azoles structure and the situation with epoxy group(ing) are more specifically explained.
As the structure more specifically of the compound with epoxy group(ing) of general formula (I) expression, the structure of No.11～18 below for example can enumerating out; As the concrete structure of the compound with epoxy group(ing) of general formula (II) expression, can enumerate out the structure of following No.19; Likewise,, the compound of No.20-1 can be enumerated out,, the compound of No.20-2 can be enumerated out as the compound of general formula (IV) as the compound of general formula (III) expression.But the present invention does not receive any restriction of following structure.
In addition; The compound method of the compound with epoxy group(ing) (being also referred to as epoxy compounds) of general formula (I) expression can obtain through compound with phenol property hydroxyl (being also referred to as phenolic compound) and the epichlorohydrin reaction that in solvent, in the presence of alkali, makes general formula (I) expression shown in following reaction formula (C).
Reaction formula (C)
In addition, general formula (II), (III) or (IV) compound with epoxy group(ing) (being also referred to as epoxy compounds) of expression also can obtain through the compound with phenol property hydroxyl (being also referred to as phenolic compound) and the epichlorohydrin reaction that in solvent, in the presence of alkali, make each self-corresponding general formula (II), (III) or (IV) represent.
Curable epoxy resin composition of the present invention can use known other epoxy compounds as epoxy compounds using the compound (being also referred to as phenolic compound) with phenol property hydroxyl of the present invention, being the phenolic compound (for example aforesaid compound No.10-2) of phenolic compound (for example aforesaid compound No.10-1), general formula (IV) expression of phenolic compound (for example aforesaid compound No.9), general formula (III) expression of phenolic compound (for example aforesaid compound No.1～8), general formula (II) expression of general formula (I) expression during as solidifying agent; Certainly using the compound (being also referred to as epoxy compounds) with epoxy group(ing) of the present invention, when being the epoxy compounds (for example aforesaid compound No.20-2) of epoxy compounds (for example aforesaid compound No.20-1), general formula (IV) expression of epoxy compounds (for example aforesaid compound No.19), general formula (III) expression of epoxy compounds (for example aforesaid compound No.11～18), general formula (II) expression of general formula (I) expression, also can use known other epoxy compounds as epoxy compounds.
As the epoxy compounds that uses in the curable epoxy resin composition of the present invention, do not have special restriction, can use known aromatic epoxy compound, alicyclic epoxide compound, aliphatic epoxy compound etc.As aromatic epoxy compound, can enumerate out for example quinhydrones, Resorcinol, dihydroxyphenyl propane, Bisphenol F, 4,4 '-dihydroxybiphenyl, phenolic varnish, tetrabromo-bisphenol, 2; Two (the 4-hydroxy phenyls)-1,1,1 of 2-; 3,3, the glycidyl ether compound of polyphenol such as 3-HFC-236fa.As alicyclic epoxide compound, the polyglycidyl ether that can enumerate out the polyvalent alcohol of the alicyclic ring with at least more than one perhaps carries out the compound that contains epoxy cyclohexane or cyclopentane epoxide that epoxidation obtains through the compound that uses oxygenant will contain tetrahydrobenzene or cyclopentenes ring.Hydrogenated Bisphenol A 99 diglycidylether, 3 for example, 4-epoxycyclohexyl methyl-3,4-epoxycyclohexyl carboxylicesters, 3; 4-epoxy-1-methylcyclohexyl-3,4-epoxy-1-methyl hexane carboxylicesters, 6-methyl-3,4-epoxycyclohexyl methyl-6-methyl-3; 4-epoxycyclohexane carboxylate, 3,4-epoxy-3-methyl cyclohexane ylmethyl-3,4-epoxy-3-methylcyclohexanecarboxylic acid ester, 3; 4-epoxy-5-methyl cyclohexane ylmethyl-3,4-epoxy-5-methylcyclohexanecarboxylic acid ester, two (3,4-epoxycyclohexyl methyl) adipic acid ester, methylene-bis (3; The 4-epoxy cyclohexane), 2; Two (3, the 4-epoxycyclohexyl) propane of 2-, Dicyclopentadiene (DCPD) diepoxide, ethylenebis (3, the 4-epoxycyclohexane carboxylate), epoxy di-2-ethylhexyl hexahy-, epoxy di-2-ethylhexyl etc.As the aliphatic epoxy compound, can enumerate out the poly glycidyl ester of polyglycidyl ether, the aliphatic long-chain polyprotonic acid of aliphatic polyol or its alkylene oxide adducts, the vinyl polymerization institute synthetic homopolymer through glycidyl acrylate or glycidyl methacrylate, the vinyl polymerization institute synthetic multipolymer through glycidyl acrylate or glycidyl methacrylate and other vinyl monomer etc.As representational compound; Can enumerate out 1; 4-butanediol diglycidyl ether, 1, the polyglycidyl ether of the glycidyl ether of polyvalent alcohols such as four glycidyl ethers of the triglycidyl ether of 6-hexanediol diglycidyl ether, glycerine, the triglycidyl ether of TriMethylolPropane(TMP), Sorbitol Powder, six glycidyl ethers of Dipentaerythritol, the diglycidylether of polyoxyethylene glycol, the diglycidylether of W 166 and the polyether glycol that obtains through the epoxy alkane of addition more than a kind or 2 kinds on aliphatic polyols such as Ucar 35, TriMethylolPropane(TMP), glycerine, the 2-glycidyl ester of aliphatic long-chain diprotic acid.In addition, can also enumerate out monoglycidyl ether and phenol, cresols, butylphenol, or the glycidyl ester of the monoglycidyl ether of the Aethoxy Sklerol that obtains through addition epoxy alkane on them, higher fatty acid, epoxidised soybean oil, epoxidation octyl stearate, epoxidation butyl stearate, epoxidized polybutadiene etc. of aliphatics higher alcohols.
In curable epoxy resin composition of the present invention, the usage quantity of solidifying agent does not have special restriction, and total epoxy mole number of epoxy compounds is 0.9/1.0～1.0/0.9 with the ratio of functional group's number of solidifying agent usually; When using epoxy compounds of the present invention as epoxy resin, in curable epoxy resin composition of the present invention, the consumption of solidifying agent preferably contains 30 quality %～80 quality %.In addition, because the substituted solidifying agent of fluorine can form the low epoxy resin of water-intake rate, thus preferred, but because the common price height of fluorine substitution compound, suitably select according to purposes so comprise other characteristic value etc.
In addition; Curable epoxy resin composition of the present invention can use known other solidifying agent as solidifying agent using epoxy compounds of the present invention, being the epoxy compounds (for example aforesaid compound No.20-2) of epoxy compounds (for example aforesaid compound No.20-1), general formula (IV) expression of epoxy compounds (for example aforesaid compound No.19), general formula (III) expression of epoxy compounds (for example aforesaid compound No.11～18), general formula (II) expression of general formula (I) expression during as epoxy compounds; Certainly using phenolic compound of the present invention, being the phenolic compound (for example aforesaid compound No.10-2) of phenolic compound (for example aforesaid compound No.10-1), general formula (IV) expression of phenolic compound (for example aforesaid compound No.9), general formula (III) expression of phenolic compound (for example aforesaid compound No.1～8), general formula (II) expression of general formula (I) expression during, also can use known other solidifying agent as solidifying agent as solidifying agent.
Through with other solidifying agent combination use, can expect viscosity, curing characteristics to resulting solidification compound or solidify after rerum natura etc. control.As other solidifying agent, can enumerate out potential curing agent, polyamine compounds, polyphenolic substance and positively charged ion is light trigger etc.
As potential curing agent, can enumerate out Dyhard RU 100, hydrazides, imidazolium compounds, amine affixture, sulfosalt, salt, ketoimine, acid anhydrides, tertiary amine etc.These potential curing agents can provide the single-liquid type solidification compound, and so operation easily is preferred.
As acid anhydrides, can enumerate out for example Tetra hydro Phthalic anhydride, trimellitic acid 1,2-anhydride, PMA, Tetra Hydro Phthalic Anhydride, hexahydrophthalic anhydride, maleic anhydride, succinyl oxide, 2,2-two (3; 4-dicarboxyl phenyl)-1,1,1; 3,3,3-hexafluoropropane dianhydride etc.
As polyamine compounds, can enumerate out for example aliphatic polyamines such as quadrol, Diethylenetriamine, three second tetramines, menthene diamines (menthene diamine), isophorone diamine, two (4-amino-3-methylcyclohexyl) methane, two (amino methyl) hexanaphthene, 3; Two (the 3-aminopropyls) 2,4,8 of 9-; Alicyclic polyamines such as 10-four oxaspiros [5,5] undecane, m-xylene diamines etc. have the fatty amine of aromatic ring; Mphenylenediamine, 2, two (4-aminophenyl) propane of 2-, diaminodiphenyl-methane, diamino diphenyl sulfone, α, α-two (4-aminophenyl)-to diisopropyl benzene, 2; Two (the 4-aminophenyls)-1,1,1 of 2-; 3,3, aromatic polyamines such as 3-HFC-236fa.
As polyphenolic substance, can enumerate out for example phenol phenolic varnish, o-Hydroxytoluene Novolac, tert.-butyl phenol phenolic varnish, Dicyclopentadiene (DCPD) cresols, terpenes biphenol, terpenes two catechols, 1,1; 3-three (3-tertiary butyl-4-hydroxy-6-aminomethyl phenyl) butane, fourth fork base two (3-tertiary butyl-4-hydroxy-6-aminomethyl phenyl), 2, two (the 4-hydroxy phenyls)-1,1 of 2-; 1; 3,3,3-HFC-236fa etc.The phenol phenolic varnish are owing to electrical characteristic, the physical strength of resulting epoxy resin are fit to veneer sheet, so preferred.
The cationic light trigger that uses among the present invention is meant the compound that can discharge the material that causes cationoid polymerisation through the energy line irradiation, and preferred especially compound is to discharge double salt or its verivate of lewis acidic salt through irradiation.As the representative example of this compound, can enumerate out general formula [A]
M+[B]
M-Represented positively charged ion and anionic salt.
Wherein, positively charged ion [A]
M+Be preferably, its structure can be used for example general formula [(R
1)
aQ]
M+Expression.
In addition, wherein, R
1The expression carbonatoms is 1～60 and can comprises the organic group of several atoms except that carbon atom.A is 1～5 integer.A R
1Can be the same or different independently of one another.In addition, preferred wherein at least 1 is for having the aforesaid organic group of aromatic ring.Q is atom or the atomic group that is selected among S, N, Se, Te, P, As, Sb, Bi, O, I, Br, Cl, F, the N=N.In addition, as positively charged ion [A]
M+In the valency of Q when being made as q, must satisfy the relation (wherein the valency of N=N being used as 0 handles) of m=a-q.
In addition, negatively charged ion [B]
M-Be preferably halide complex, its structure can be used for example general formula [LX
b]
M-Represent.
In addition, wherein, L is as the metal of the central atom of halide complex or semi-metal (Metalloid), is B, P, As, Sb, Fe, Sn, Bi, Al, Ca, In, Ti, Zn, Sc, V, Cr, Mn, Co etc.X is a halogen atom.B is 3～7 integer.In addition, as negatively charged ion [B]
M-In the valency of L when being made as p, must satisfy the relation of m=b-p.
As the represented negatively charged ion [LX of above-mentioned general formula
b]
M-Specific examples, can enumerate out a tetrafluoro borate (BF
4)
-, hexafluorophosphate (PF
6)
-, hexafluoro antimonate (SbF
6)
-, hexafluoro arsenate (AsF
6)
-, hexa chloro-antimonate (SbCl
6)
-Deng.
In addition, negatively charged ion [B]
M-Can preferably use [LX
B-1(OH)]
M-The negatively charged ion of represented structure.The definition of L, X, b is the same.In addition, as operable other negatively charged ion, can enumerate out high chloro acid ion (ClO
4)
-, trifluoromethyl sulfurous acid ion (CF
3SO
3)
-, fluoro azochlorosulfonate acid ion (FSO
3)
-, toluenesulphonic acids negatively charged ion, trinitrobenzenesulphonic acid negatively charged ion etc.
In the present invention, in such salt, the aromatic series salt that uses following (i)～(iii) is effective especially.These salt can use a kind separately, perhaps can mix and use more than 2 kinds.
I) aryl diazonium salts such as phenyl diazonium hexafluorophosphate, 4-p-methoxy-phenyl diazonium hexafluoro antimonate, 4-aminomethyl phenyl diazonium hexafluorophosphate
Ii) diaryl group iodized salt such as phenylbenzene iodine hexafluoro antimonate, two (4-aminomethyl phenyl) iodine hexafluorophosphate, two (4-tert-butyl-phenyl) iodine hexafluorophosphate
Iii) triphenyl sulphur hexafluoro antimonate, three (4-p-methoxy-phenyl) sulphur hexafluorophosphate, phenylbenzene-4-sulfo-Phenoxyphenyl sulphur hexafluoro antimonate, phenylbenzene-4-sulfo-Phenoxyphenyl sulphur hexafluorophosphate, 4; 4 '-two (phenylbenzene sulfonium base (sulfonio)) phenyl thioether-two-hexafluoro antimonate, 4; 4 '-two (phenylbenzene sulfonium base) phenyl sulfide-pairs-hexafluorophosphate, 4; 4 '-two [two (beta-hydroxy oxyethyl group) phenyl sulfonium base] phenyl thioether-two-hexafluoro antimonate, 4,4 '-two [two (beta-hydroxy oxyethyl group) phenyl sulfonium base] phenyl sulfide-pairs-hexafluorophosphate, 4-[4 '-(benzoyl-) thiophenyl] phenyl-two-(4-fluoro phenyl) sulphur hexafluoro antimonate, 4-[4 '-(benzoyl-) thiophenyl] phenyl-two-triaryl sulfonium salts such as (4-fluoro phenyl) sulphur hexafluorophosphate etc.
In addition, as other preferred compound, can also enumerate out (η
5-2,4-cyclopentadiene-1-yl) [(1,2; 3; 4,5,6;-η)-(1-methylethyl) benzene]-iron such as iron-hexafluorophosphate-aromatic hydrocarbons complex compound, and the mixture of silane alcohols such as aluminium complex such as aluminium tris(acetylacetonate), three (ethyl acetone acetate (ethylacetonatoacetato)) aluminium, three (salicylic aldehyde) aluminium and tri-phenyl-silane alcohol etc.
Wherein, from the viewpoint of practicality and light sensitivity, optimization aromatic salt compounded of iodine, aromatic series sulfosalt, iron-aromatic hydrocarbons complex compound.
These light triggers can use a kind in the known Photoepolymerizationinitiater initiaters such as phenylformic acid system or tertiary amine system or make up and use more than 2 kinds.Light trigger preferably comprises 0.1～30 weight % in compsn of the present invention.If less than 0.1 weight %, then might can not obtain additive effect, if more than 30 weight %, then the physical strength of cured article might reduce.
Employed light source in the polymerization during as the use light trigger; Can use known light sources such as high pressure mercury vapour lamp, metal halide lamp, xenon lamp; Through irradiation ultraviolet radiation, electron beam, X ray, radioactive rays, high frequency isoreactivity energy-ray; Discharge Lewis acid from above-mentioned light trigger, thereby can make above-mentioned epoxy compounds performance effect.As these light sources, the light source with the wavelength below the 400nm is effective.
Curable epoxy resin composition solidified method as the solidifying agent (phenolic compound) that has used general formula of the present invention (I), general formula (II), general formula (III) or general formula (IV) expression; Can adopt the curing of any existing known epoxy resin, can be to use curing that solidifying agent carries out, utilize curing that curing catalysts carries out through auto-polymerization, use photocuring that light trigger carries out, use curing catalyst control curing speed etc. through mixing.
In addition, as required, preferably use sphere-packing agent such as fibrous fillers such as spun glass, aluminium borate whisker, boron nitride crystal whisker and silicon oxide, aluminum oxide.Preferably suitably select the length and the long-width ratio of the y direction of fibrous filler, the spherical shape that sphere-packing agent preferable particle size is less according to purposes.
The curable epoxy resin composition of the invention described above can be through forming varnish with suitable organic solvents such as propylene glycol monomethyl ethers with its dilution; With its coating and be immersed on the porous glass base materials such as glass non-woven fabrics, glass woven fabric, and heat this ordinary method and make preimpregnation material (prepreg).In addition, many these preimpregnation materials are overlapping, obtain veneer sheet.Overlapping Copper Foil on face of this laminar structure or two faces heats it under normal condition then and pressurizes, and can access the glass fiber reinforced epoxy resin copper clad laminate thus.Go up to form circuit at this copper clad laminate (inner plating), then Copper Foil is carried out etch processes, overlapping preimpregnation material and Copper Foil at least one face of inner plating then, and at for example 170 ℃, 40kg/cm
2Pressure under to its heating and pressure treatment of carrying out 90 minutes, can make multi-ply wood through this ordinary method.In addition, on this copper clad laminate or this multi-ply wood, form through hole, carry out the through hole plating, form the circuit of regulation then, can make printed substrate through this ordinary method.
Curable epoxy resin composition of the present invention can be used for various electronics and electric materials such as the employed copper clad laminate of foregoing circuit substrate, preimpregnation material, printed substrate, sealing material, mould material, caking agent, electrical insulating coating; Coating (powder coating, anticorrosive coating etc.); Caking agent; The various uses of existing known epoxy resin such as building materials.
Then, novel benzo
azole compounds to formula (V) expression describes.
[in the formula, Y
1Expression Sauerstoffatom or sulphur atom.Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different.N representes 0～2 integer.A
1The substituting group that expression has the substituting group of phenol property hydroxyl or has epoxy group(ing).]
In logical formula V, those with record in the substituting group of phenol property hydroxyl, the substituting group with epoxy group(ing) and the above-mentioned general formula (I) are identical, preferably also identical.
Above-mentioned novel cpd has the situation of phenol property hydroxyl, is meant A
1Situation for substituting group (also comprising phenylol itself) with phenol property hydroxyl; Have the situation of epoxy group(ing), be meant A
1Situation for substituting group (also comprising epoxy group(ing) itself) with epoxy group(ing).
Above-mentioned novel cpd is under the situation with phenol property hydroxyl; Structure can be enumerated out the structure of above-claimed cpd No.2 for example and 3 more specifically; Above-mentioned novel cpd has under the situation of epoxy group(ing), and structure more specifically can be enumerated out the for example structure of above-claimed cpd NO.11～13.But the present invention does not receive any qualification of following structure.
In addition, above-mentioned novel cpd has the method that compound method under the situation of epoxy group(ing) can be used for example above-mentioned record at the situation with phenol property hydroxyl and above-mentioned novel cpd.
Above-mentioned novel cpd can also be used for cementability epoxy composite, low linear expansion pre-soaked resin etc. except being used for the above-mentioned curable epoxy resin composition as curing agent for epoxy resin or epoxy resin.
Then, novel benzo
azole compounds to formula (VI) expression describes.
[in the formula, Y
1Expression Sauerstoffatom or sulphur atom.Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different.N representes 0～2 integer.A
1The substituting group that expression has the substituting group of phenol property hydroxyl or has epoxy group(ing).]
In general formula (VI), have phenol property hydroxyl substituting group, have a record in substituting group and the above-mentioned general formula (I) of epoxy group(ing) those are identical, preferably also identical.
Above-mentioned novel cpd has the situation of phenol property hydroxyl, is meant A
1Situation for substituting group (also comprising phenylol itself) with phenol property hydroxyl; Have the situation of epoxy group(ing), be meant A
1Situation for substituting group (also comprising epoxy group(ing) itself) with epoxy group(ing).
As the concrete structure of above-mentioned novel cpd, for example when having epoxy group(ing), can enumerate out the structure of above-claimed cpd No.14.But the present invention does not receive any qualification of following structure.
In addition, above-mentioned novel cpd has the method that compound method under the situation of epoxy group(ing) for example can be used above-mentioned record at the situation with phenol property hydroxyl and above-mentioned novel cpd.
Azole compounds likewise for the novel benzo
that above-mentioned general formula (VI) expression novel cpd and above-mentioned logical formula V are represented; Except being used for the above-mentioned curable epoxy resin composition, can also be used for cementability epoxy composite, low linear expansion pre-soaked resin etc. as curing agent for epoxy resin or epoxy resin.
Embodiment
Through embodiment the present invention is at length explained.But the present invention does not receive any qualification of embodiment.
In addition, embodiment 1～10 expression phenolic compound and the synthetic example of having used the epoxy compounds of this phenolic compound.According to the proportioning of following [table 1] and [table 2] record, preparation contains the curable epoxy resin composition of the present invention of this epoxy compounds.In addition, comparative example 1～5 expression is according to the proportioning of [table 3] record, and preparation contains the comparison curable epoxy resin composition of comparative compound.Use this curable epoxy resin composition of gained maybe should compare curable epoxy resin composition; Through following method of manufacture; Make test film A～C; According to following TP, chemical reagent resistance test, second-order transition temperature, linear expansivity, tensile strength, elongation, scolding tin thermotolerance, heat-resisting cyclicity are made an experiment.The result is shown in [table 1]～[table 3].The solidifying agent 1～3 that uses is as follows.
Solidifying agent 1
Solidifying agent 2
The OH equivalent of solidifying agent 2 is 270g/eq.
Solidifying agent 3
[embodiment 1 (the synthetic example of phenolic compound NO.2 and the synthetic example of having used this compound N epoxy compounds NO.12 o.2)]
Method according to following record obtains epoxy compounds No.12 from the phenolic compound No.2 that following method obtains.
(1) (the synthetic example of phenolic compound NO.2)
Under nitrogen gas stream; In 4 mouthfuls of flasks of 200mL; Add 21.624g (0.10mol) 3, N-cyclohexyl-2-Pyrrolidone of 3 '-dihydroxybiphenyl amine, 29.42g (0.21mol) 4-fluorinated acid and 65mL carries out 24 hours amidate action under 130-140 ℃.Afterwards, be warmed up to 260 ℃, kept 2 hours.During this time, append the 4-fluorinated acid that adds 5g, reacted 24 hours down at 260 ℃ again.After the cooling; Filter and take out the yellow crystals of separating out; Use the 50mL methanol wash; Obtain 2,2 ' of 28.4g-two (4-fluoro phenyl) two benzos
azoles.
Then; Under nitrogen gas stream; In 4 mouthfuls of flasks of 100mL, add 6.36g (0.015mol) 2,2 '-two (4-fluoro phenyl) two benzos
azoles; 8.253g (0.075mol) quinhydrones; 7.69g (0.06mol) N-Methyl pyrrolidone of salt of wormwood, 40mL (NMP) and 25mL toluene, on one side 130 ℃ of refluxed (reflux) 2 hours, on one side with distilled water except that to system.Afterwards, heat up, on one side piptonychia benzene, kept 6 hours down at 160 ℃ on one side.Then, reacted 3 hours down, obtain the yellow reaction crude product at 185 ℃.This reacting coarse product is put in the 800mL water, dripped diluted hydrochloric acid aqueous solution again so that pH=7.After the neutralization, in water, stirred 2 hours, filter and take out, 150 ℃ of following drying under reduced pressure 2 hours, obtain phenolic compound, promptly o.2 compound N is 8.72g.
(2) (the synthetic example of epoxy compounds No.12)
Under nitrogen gas stream, in 3 mouthfuls of flasks of 50mL, add compound N that 2.0g (0.0033mol) (1) obtains o.2,0.264g (0.0066mol) NaOH, 10g water and 10.0g DMSO 99.8MIN. (DMSO), be warmed up to 60 ℃, stir and make its dissolving.Afterwards, drip 1.647g (0.007mol) epoxy chloropropane, kept 3 hours down at 80 ℃.After the cooling, the yellow epoxide that leaching is separated out is with 100mL water, 100mL methanol wash.Through 150 ℃ of following drying under reduced pressure 2 hours, obtain epoxy compounds, promptly o.12 compound N is 2.38g.Fig. 2 representes the compound N IR spectrogram o.12 that obtains.
The compound N of gained epoxy equivalent (weight) o.12 is 358g/eq.
[embodiment 2 (the synthetic example of phenolic compound No.3 and the synthetic example of having used this compound N epoxy compounds No.13 o.3)]
Method according to following record obtains epoxy compounds No.13 from the phenolic compound No.3 that following method obtains.
(1) (the synthetic example of phenolic compound No.3)
Under nitrogen gas stream; In 4 mouthfuls of flasks of 200mL; Add 21.624g (0.10mol) 3, N-cyclohexyl-2-Pyrrolidone of 3 '-dihydroxybiphenyl amine, 29.42g (0.21mol) 4-fluorinated acid and 65mL carries out 24 hours amidate action under 130-140 ℃.Afterwards, be warmed up to 260 ℃, kept 2 hours.During this time, append the 4-fluorinated acid that adds 5g, reacted 24 hours down at 260 ℃ again.After the cooling; Filter and take out the yellow crystals of separating out; Use the 50mL methanol wash; Obtain 2,2 ' of 28.4g-two (4-fluoro phenyl) two benzos
azoles.
Then; Under nitrogen gas stream; In 4 mouthfuls of flasks of 100mL, add 6.36g (0.015mol) 2,2 '-two (4-fluoro phenyl) two benzos
azoles; 8.253g (0.075mol) Resorcinol; 7.69g (0.06mol) N-Methyl pyrrolidone of salt of wormwood, 40mL (NMP) and 25mL toluene, on one side 130 ℃ of refluxed (reflux) 2 hours, on one side with distilled water except that to system.Afterwards, heat up, on one side piptonychia benzene, kept 6 hours down at 160 ℃ on one side.Then, reacted 3 hours down, obtain the yellow reaction crude product at 185 ℃.This reacting coarse product is put in the 800mL water, dripped diluted hydrochloric acid aqueous solution again so that pH=7.After the neutralization, in water, stirred 2 hours, filter and take out, 150 ℃ of following drying under reduced pressure 2 hours, obtain phenolic compound, promptly o.3 compound N is 8.72g.
(2) (the synthetic example of epoxy compounds No.13)
Under nitrogen gas stream, in 3 mouthfuls of flasks of 50mL, add compound N that 2.0g (0.0033mol) (1) obtains o.3,0.264g (0.0066mol) NaOH, 10g water and 10.0g DMSO 99.8MIN. (DMSO), be warmed up to 60 ℃, stir and make its dissolving.Afterwards, drip 1.647g (0.007mol) epoxy chloropropane, kept 3 hours down at 80 ℃.After the cooling, the yellow epoxide that leaching is separated out is with 100mL water, 100mL methanol wash.Through 150 ℃ of following drying under reduced pressure 2 hours, obtain epoxy compounds, promptly o.13 compound N is 2.38g.Fig. 3 representes the compound N IR spectrogram o.13 that obtains.The compound N of gained epoxy equivalent (weight) o.13 is 358g/eq.
[embodiment 3 (the synthetic example of phenolic compound No.1 and the synthetic example of having used this compound N epoxy compounds No.11 o.1)]
According to the identical method of embodiment 1 record, obtain epoxy compounds No.11 from following phenolic compound No.1.In addition, phenolic compound No.1 basis is synthetic with the identical method of embodiment 1 record.
The compound N of gained epoxy equivalent (weight) o.11 is 266g/eq.
[embodiment 4 (the synthetic example of phenolic compound No.7 and the synthetic example of having used this compound N epoxy compounds No.17 o.7)]
According to the identical method of embodiment 1 record, obtain epoxy compounds No.17 from following phenolic compound No.7.In addition, phenolic compound No.7 basis is synthetic with the identical method of embodiment 1 record.
The compound N of gained epoxy equivalent (weight) o.17 is 300g/eq.
[embodiment 5 (the synthetic example of phenolic compound No.4 and the synthetic example of having used this compound N epoxy compounds No.14 o.4)]
According to the method for following record, the phenolic compound No.4 that obtains from following method obtains epoxy compounds No.14.
(1) (the synthetic example of phenolic compound No.4)
Under nitrogen gas stream, in 4 mouthfuls of flasks of 200mL, add 39.23g (0.1mol) 2,2 pairs of (3-amino-4-hydroxy phenyl HFC-236fa) and 44.99g (0.21mol) PHB phenylesters, be heated to 150 ℃.With reducing pressure in the system,,, kept 3 hours Yi Bian be warmed up to 180 ℃ Yi Bian heat up in a steamer phenol.After getting back to normal atmosphere,, carry out 20 hours closed loop dehydration reactions with being warmed up to 240 ℃ in the system.With 100gNMP dissolving, reaction soln to be put in the 1000mL water, redeposition takes out crystal, and is last with ion exchanged water and methanol wash, and crystal 120 ℃ of dryings 3 hours down, is obtained phenolic compound, and promptly o.4 compound N is 50g (yield 83.8%).Fig. 4 representes the compound N IR spectrogram o.4 that obtains.
(2) (the synthetic example of epoxy compounds No.14)
O.4, the compound N that 20g aforementioned (1) is obtained is dissolved in the 200mL epoxy chloropropane, and 48% sodium hydroxide through 5.59g carries out esterification and closed loop, obtains compound N o.14.Fig. 5 representes the compound N IR spectrogram o.14 of gained.
The compound N of gained epoxy equivalent (weight) o.14 is 341g/eq.
[embodiment 6 (the synthetic example of phenolic compound No.5 and the synthetic example of having used this compound N epoxy compounds No.15 o.5)]
According to the identical method of embodiment 1 record, obtain epoxy compounds No.15 from following phenolic compound No.5.In addition, phenolic compound No.5 basis is synthetic with the identical method of embodiment 1 record.
The compound N of gained epoxy equivalent (weight) o.15 is 229g/eq.
[embodiment 7 (the synthetic example of phenolic compound No.6 and the synthetic example of having used this compound N epoxy compounds No.16 o.6)]
According to the identical method of embodiment 1 record, obtain epoxy compounds No.16 from following phenolic compound No.6.In addition, phenolic compound No.6 basis is synthetic with the identical method of embodiment 1 record.
The compound N of gained epoxy equivalent (weight) o.16 is 254g/eq.
[embodiment 8 (the synthetic example of phenolic compound No.8 and the synthetic example of having used this compound N epoxy compounds No.18 o.8)]
According to the identical method of embodiment 1 record, obtain epoxy compounds No.18 from following phenolic compound No.8.In addition, phenolic compound No.8 basis is synthetic with the identical method of embodiment 1 record.
The compound N of gained epoxy equivalent (weight) o.18 is 316g/eq.
[embodiment 9 (the synthetic example of phenolic compound No.9 and the synthetic example of having used this compound N epoxy compounds No.19 o.9)]
According to the identical method of embodiment 1 record, the phenolic compound No.9 that obtains from following method obtains epoxy compounds No.19.
The compound N of gained epoxy equivalent (weight) o.19 is 338g/eq.
(the synthetic example of phenolic compound No.9)
5.46g (0.03mol) 5-hydroxyl m-phthalic acid, 5.91g (0.03mol) amidol, 9.31g (0.03mol) triphenyl phosphite, 2.54g (0.06mol) lithium chloride, 37.8gN-SL 1332 (NMP) and 9.45g pyridine are added together, reacted 3 hours down at 100 ℃.After the reaction,, filter, obtain crude product with about 1.5L acetone redeposition; With about 300ml acetone boiling washing after 30 minutes, filtration was 150 ℃ of following drying under reduced pressure 3 hours; Then, through under 260 ℃, 10 hours vacuum-drying carries out closed loop, obtain thus o.9 as the compound N of phenolic compound.
[embodiment 10 (the synthetic example of phenolic compound No.10-1 and the synthetic example of having used this compound N epoxy compounds No.20-1 o.10-1)]
Through with the identical method of embodiment 1 record, the phenolic compound No.10-1 that obtains from following method obtains epoxy compounds No.20-1.
The compound N of gained epoxy equivalent (weight) o.20-1 is 336g/eq.
(the manufacturing example of phenolic compound No.10-1)
With 5.46g (0.03mol) 5-hydroxyl m-phthalic acid, 6.39g (0.03mol) 4; 6-diamyl Resorcinol dihydrochloride, 9.31g (0.03mol) triphenyl phosphite, 2.54g (0.06mol) lithium chloride, 37.8gN-SL 1332 (NMP) and 9.45g pyridine add together, react 3 hours down at 100 ℃.After the reaction,, filter with about 1.5L acetone redeposition; Obtain crude product, after 30 minutes, filter with about 300ml acetone boiling washing; 150 ℃ of following drying under reduced pressure 3 hours; Then, through under 260 ℃, 10 hours vacuum-drying carries out closed loop, obtain thus o.10-1 as the compound N of phenolic compound.
[comparative example 1～5 (containing the preparation of the curable epoxy resin composition of comparison epoxy compounds 1～5)]
With the comparison epoxy compounds 1～5 of [table 3] record, curable epoxy resin composition is compared in preparation and the foregoing description is likewise made test film, estimates.The result is shown in [table 3].
Compare epoxy compounds 1
Relatively the epoxy equivalent (weight) of epoxy compounds 1 is 136g/eq.
Compare epoxy compounds 2
Relatively the epoxy equivalent (weight) of epoxy compounds 2 is 170g/eq.
Compare epoxy compounds 3
Relatively the epoxy equivalent (weight) of epoxy compounds 3 is 126g/eq.
Compare epoxy compounds 4
Relatively the epoxy equivalent (weight) of epoxy compounds 4 is 180g/eq.
Compare epoxy compounds 5
Relatively the epoxy equivalent (weight) of epoxy compounds 5 is 162g/eq.
[TP]
(1) manufacturing of test film
Test film A: thick curable epoxy resin composition or the comparison curable epoxy resin composition of coating 200 μ m distributes on the PET film that the thick sur-face peeling of 38 μ m was handled; In heated oven; Drying is 10 minutes under 130 ℃, makes the resin B rankization, makes dry film.In 90 ℃, 10 minutes, this dry film is fitted on the glass substrate that sur-face peeling handled,, peel off the PET film afterwards, the B b stage resin b is transferred on the glass substrate so that the resin face contacts with glass surface through the vacuum layer platen press.With transfer printing the glass substrate of B b stage resin b put into heated oven, under 150 ℃, in 1 hour, make the resin completely solidified, get back to room temperature after, peel off resin from glass substrate, thereby obtain completely crued resin film (test film A).
Test film B: on the thick tarnish of printed base plate of 12 μ m with electrolytic copper foil; Be coated with thick curable epoxy resin composition of 100 μ m or comparison curable epoxy resin composition; In heated oven; Drying is 10 minutes under 130 ℃, makes the Copper Foil that has resin that makes the resin B rankization.With thick glass fiber reinforced epoxy resin two sides substrate (FR-4) of 0.1mm as core; Be fitted on the two sides through the Copper Foil of vacuum pressure method for making (lamination is illustrated in fig. 1 shown below) this tape tree fat; Make the resin completely solidified, thereby obtain testing substrate (test film B).
Test film C: use-testing sheet B, it is 70 μ m that manufacturing has electrode diameter, interelectrode distance is the foursquare wiring substrate of 40mm of the electrode of 120 μ m.It is that 70 μ m, interelectrode distance are the LSI chip of length * wide * height=8.5 * 8.5 * 0.06mm of the au bump electrode of 120 μ m that manufacturing has electrode diameter; The curable epoxy resin composition of each embodiment or comparative example or comparison curable epoxy resin composition are applied to around the electrode of LSI chip; Afterwards the LSI chip is arranged on the wiring substrate; So that the electrode of substrate and chip contacts; Put into heated oven then, under 150 ℃, in 1 hour, make the resin completely solidified, thereby obtain test film C.
(2) chemical reagent resistance test
Use-testing sheet A is with the cotton rod that soaked NMP (N-Methyl pyrrolidone), wipe test sheet surface, the wiping number of times when determination test sheet surface reaches damage.
(3) second-order transition temperature
Use-testing sheet A uses cutter to be configured as 5 * 50mm size, through the DMS-6100 of SII NanoTechnology manufactured, measures dynamic viscoelastic, with the peaked temperature of expression Tan δ as second-order transition temperature.
(4) linear expansivity
Use-testing sheet A uses cutter to be configured as 5 * 50mm size, through the TMA/SS6000 of SII NanoTechnology manufactured, measures the linear expansion curve of heating.Calculate linear expansivity from the elongation of 40～100 ℃ scopes.
(5) tensile strength, elongation
Use-testing sheet A measures according to JIS-K7127 (use-testing sheet model 5).
(6) scolding tin thermal test
Use-testing sheet B is configured as the 40mm square, in being adjusted into 288 ℃ solder bath, suspended 1 minute, inspection have or not from the teeth outwards peel off etc. unusual etc.From solder bath, take out test film, at room temperature leave standstill 1 minute after, repeat same operation 10 times, inspection can be born several cycles.
(7) heat-resisting cyclicity test
Use-testing sheet C after making an experiment according to IPC-D-275 (test conditions E), observes the change in resistance of outward appearance, check circuit, judges to have or not abnormal conditions such as broken string, distribution fracture, loose contact.
[table 1]
| ? | |
Embodiment 2 | Embodiment 3 | |
Embodiment 5 |
| Compound N o.12 | 10g | ? | ? | ? | ? |
| Compound N o.13 | ? | 10g | ? | ? | ? |
| Compound N o.11 | ? | ? | 10g | ? | ? |
| Compound N o.17 | ? | ? | ? | 10g | ? |
| Compound N o.14 | ? | ? | ? | ? | 10g |
| Solidifying |
1.00g | 1.00g | 1.34g | 1.19g | 1.05g |
| Solidifying agent 2 | ? | ? | ? | ? | ? |
| Solidifying agent 3 | ? | ? | ? | ? | ? |
| Triphenylphosphine | ? | ? | ? | ? | ? |
| NMP | 11.00g | 11.00g | 11.34g | 11.19g | 11.05g |
| Chemical reagent resistance | More than 100 times | More than 100 times | More than 100 times | More than 100 times | More than 100 times |
| Second-order transition temperature | 180℃ | 175℃ | 195℃ | 160℃ | 180℃ |
| Linear expansivity | 5.0ppm | 5.5ppm | 3.0ppm | 10.0ppm | 6.0ppm |
| Tensile strength | 90MPa | 90MPa | 80MPa | 105MPa | 95MPa |
| Elongation | 5.0％ | 5.5％ | 3.0％ | 8.0％ | 6.0％ |
| The scolding |
10 |
10 |
10 |
10 |
10 times |
| Heat-resisting cyclicity | No abnormal | No abnormal | No abnormal | No abnormal | No abnormal |
[0285] [table 2]
| ? | Embodiment 6 | Embodiment 7 | Embodiment 8 | Embodiment 9 | |
| Compound N o.15 | 10g | ? | ? | ? | ? |
| Compound N o.16 | ? | 10g | ? | ? | ? |
| Compound N o.18 | ? | ? | 10g | ? | ? |
| Compound N o.19 | ? | ? | ? | 10g | ? |
| Compound N o.20-1 | ? | ? | ? | ? | 10g |
| Solidifying |
? | ? | ? | ? | ? |
| Solidifying agent 2 | 11.8g | 10.6g | 8.5g | ? | ? |
| Solidifying agent 3 | ? | ? | ? | 5.0g | 5.0g |
| Triphenylphosphine | 0.65g | 0.62g | 0.56g | 0.45g | 0.45g |
| NMP | 22.45g | 21.22g | 19.06g | 15.45g | 15.45g |
| Chemical reagent resistance | More than 100 times | More than 100 times | More than 100 times | More than 100 times | More than 100 times |
| Second-order transition temperature | 185℃ | 190℃ | 160℃ | 180℃ | 190℃ |
| Linear expansivity | 15.0ppm | 12.0ppm | 18.0ppm | 5.0ppm | 5.0ppm |
| Tensile strength | 80MPa | 85MPa | 100MPa | 90MPa | 80MPa |
| Elongation | 3.0％ | 3.5％ | 4.5％ | 4.0％ | 3.0％ |
| The scolding |
10 |
10 |
10 |
10 |
10 times |
| Heat-resisting cyclicity | No abnormal | No abnormal | No abnormal | No abnormal | No abnormal |
[0287] [table 3]
| ? | Comparative example 1 | Comparative example 2 | Comparative example 3 | Comparative example 4 | Comparative example 5 |
| Compare |
10g | ? | ? | ? | ? |
| Compare epoxy compounds 2 | ? | 10g | ? | ? | ? |
| Compare epoxy compounds 3 | ? | ? | 10g | ? | ? |
| Compare |
? | ? | ? | 10g | ? |
| Compare epoxy compounds 5 | ? | ? | ? | ? | 10g |
| Solidifying |
2.62g | 2.11g | 2.83g | 1.98g | 2.20g |
| Solidifying agent 2 | ? | ? | ? | ? | ? |
| Solidifying agent 3 | ? | ? | ? | ? | ? |
| Triphenylphosphine | ? | ? | ? | ? | ? |
| NMP | 12.62g | 12.11g | 12.83g | 11.98g | 12.20g |
| Chemical reagent resistance | More than 100 times | More than 100 times | More than 100 times | More than 100 times | More than 100 times |
| Second- |
150℃ | 135℃ | 160℃ | 170℃ | 180℃ |
| Linear expansivity | 50ppm | 60ppm | 55ppm | 50ppm | 50ppm |
| Tensile strength | 80MPa | 80MPa | 85MPa | 75MPa | 70MPa |
| Elongation | 3.0％ | 4.0％ | 5.0％ | 2.5％ | 2.0％ |
| The scolding |
1 |
0 |
1 time | 2 times | 2 times |
| Heat-resisting cyclicity | Broken string, fracture, loose contact are arranged | Broken string, fracture, loose contact are arranged | Broken string, fracture, loose contact are arranged | Broken string, fracture, loose contact are arranged | Broken string, fracture, loose contact are arranged |
Through with the compound with benzo
azoles structure of the present invention as solidifying agent, or use as epoxy resin; Even do not use filler, can provide also that linear expansivity is low, the also excellent curable epoxy resin compositions of rerum natura such as tensile strength and elongation.
Claims (7)
1. curable epoxy resin composition is characterized in that: contain the compound of formula (I) expression,
In the formula, X
1And X
2Separately independently of each other, the substituting group that can represent Wasserstoffatoms identical or differently, have the substituting group of phenol property hydroxyl or have epoxy group(ing), but X
1And X
2Be not Wasserstoffatoms simultaneously, and, X
1Or X
2In any represent with formula (Ia); Y
1Expression Sauerstoffatom or sulphur atom, Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different, n representes 0～2 integer, A
1Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing),
In the said general formula (Ia), Y
1Expression Sauerstoffatom or sulphur atom, Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different, n representes 0～2 integer, A
1Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).
2. curable epoxy resin composition is characterized in that: contain the compound of formula (I) expression,
In the formula, X
1And X
2Separately independently of each other, the substituting group that can represent Wasserstoffatoms identical or differently, have the substituting group of phenol property hydroxyl or have epoxy group(ing), but X
1And X
2Be not Wasserstoffatoms simultaneously, and, X
1Or X
2In any represent with formula (Ib); Y
1Expression Sauerstoffatom or sulphur atom, Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different, n representes 0～2 integer, A
1Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing),
In the said general formula (Ib), Y
1Expression Sauerstoffatom or sulphur atom, Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different, n representes 0～2 integer, A
1Expression Wasserstoffatoms, the substituting group that has the substituting group of phenol property hydroxyl or have epoxy group(ing).
3. the curable epoxy resin composition of being put down in writing according to claim 1 or 2 is characterized in that: in the said general formula (I), and A
1It is substituting group with epoxy group(ing).
4. a veneer sheet is used solidification compound, and it has used each curable epoxy resin composition of putting down in writing in the claim 1～3.
5. cured article, it is to obtain through each curable epoxy resin composition of putting down in writing is solidified.
6. compound with formula (V) expression,
In the formula, Y
1Expression Sauerstoffatom or sulphur atom, Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z
1Can be the same or different, n representes 0～2 integer, A
1The substituting group that expression has the substituting group of phenol property hydroxyl or has epoxy group(ing).
7. compound with formula (VI) expression,
In the formula, Y
1Expression Sauerstoffatom or sulphur atom, Z
1Expression can have substituent carbonatoms be 1～8 alkyl maybe can to have substituent carbonatoms be 1～8 alkoxyl group, m representes 0～4 integer, m is 2～4 o'clock, a plurality of Z1 can be the same or different, n representes 0～2 integer, A
1The substituting group that expression has the substituting group of phenol property hydroxyl or has epoxy group(ing).
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP087843/2006 | 2006-03-28 | ||
| JP2006087843A JP4986485B2 (en) | 2006-03-28 | 2006-03-28 | Epoxy resin curable composition |
| PCT/JP2007/055106 WO2007111136A1 (en) | 2006-03-28 | 2007-03-14 | Curable epoxy resin composition |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2011100766676A Division CN102190777B (en) | 2006-03-28 | 2007-03-14 | Epoxy resin curing composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101389684A CN101389684A (en) | 2009-03-18 |
| CN101389684B true CN101389684B (en) | 2012-05-30 |
Family
ID=38541057
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2011100766676A Expired - Fee Related CN102190777B (en) | 2006-03-28 | 2007-03-14 | Epoxy resin curing composition |
| CN2007800064020A Expired - Fee Related CN101389684B (en) | 2006-03-28 | 2007-03-14 | Curable epoxy resin composition |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2011100766676A Expired - Fee Related CN102190777B (en) | 2006-03-28 | 2007-03-14 | Epoxy resin curing composition |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7763700B2 (en) |
| JP (1) | JP4986485B2 (en) |
| KR (1) | KR101344704B1 (en) |
| CN (2) | CN102190777B (en) |
| TW (1) | TWI403530B (en) |
| WO (1) | WO2007111136A1 (en) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4151573B2 (en) * | 2003-12-16 | 2008-09-17 | 東洋紡績株式会社 | Curable composition |
| US8969342B2 (en) * | 2009-03-20 | 2015-03-03 | Brandeis University | Compounds and methods for treating mammalian gastrointestinal microbial infections |
| CN102250117B (en) * | 2011-05-11 | 2013-07-24 | 华东理工大学 | Dibenzoxazine containing oxazole ring and preparation method thereof |
| CN102558605B (en) * | 2011-12-05 | 2013-12-04 | 深圳市科聚新材料有限公司 | Fire retardant, preparation method and applications thereof |
| JP6190256B2 (en) * | 2013-12-05 | 2017-08-30 | 本州化学工業株式会社 | Novel bis (hydroxyphenyl) benzoxazole compounds |
| JP6517043B2 (en) * | 2015-02-25 | 2019-05-22 | ルネサスエレクトロニクス株式会社 | Optical coupling device, method of manufacturing optical coupling device, and power conversion system |
| KR102483123B1 (en) * | 2018-10-17 | 2022-12-29 | 도요보 가부시키가이샤 | Thermally conductive resin composition |
| KR20210058569A (en) * | 2019-11-14 | 2021-05-24 | 삼성전자주식회사 | High thermal conductive epoxy compound, and composition, material for semiconductor package, molded propuct, electric and electronic device and semiconductor package including the same |
| WO2022080938A1 (en) * | 2020-10-16 | 2022-04-21 | 주식회사 엘지화학 | Polycarbonate and method for preparing same |
| KR102517520B1 (en) * | 2020-10-16 | 2023-04-04 | 주식회사 엘지화학 | Polycarbonate and method for preparing same |
| CN112625442B (en) * | 2020-12-18 | 2023-08-22 | 广东盈骅新材料科技有限公司 | Cyanate resin composition, prepreg, laminate and printed circuit board |
| CN112694714B (en) * | 2020-12-18 | 2023-01-06 | 广东盈骅新材料科技有限公司 | Epoxy resin composition, prepreg, laminate, and printed wiring board |
| CN115557899B (en) * | 2022-09-30 | 2024-03-08 | 福州大学 | Epoxy resin curing accelerator and preparation method thereof |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004010996A1 (en) * | 2002-07-29 | 2004-02-05 | Shizuoka Coffein Co., Ltd. | 1,3-azole derivative and medicinal composition containing the derivative for treatment for thombosis |
| WO2005059001A1 (en) * | 2003-12-16 | 2005-06-30 | Toyo Boseki Kabushiki Kaisha | Curable composition |
| CN1747943A (en) * | 2003-02-14 | 2006-03-15 | 出光兴产株式会社 | Heteropolycyclic compound, and coloring matter, pigment, dye, color-changing material composition and color-changing film prepared therefrom |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5270432A (en) * | 1992-04-10 | 1993-12-14 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Polybenzoxazole via aromatic nucleophilic displacement |
| DE19517448A1 (en) * | 1995-05-12 | 1996-11-14 | Thomae Gmbh Dr K | Novel benzothiazoles and benzoxazoles, medicaments containing them and their use, and processes for their preparation |
| JP2001049082A (en) | 1999-06-04 | 2001-02-20 | Nippon Kayaku Co Ltd | Epoxy resin composition, its varnish, filmy adhesive using the same and its cured substance |
| JP2001031784A (en) | 1999-07-19 | 2001-02-06 | Nippon Kayaku Co Ltd | Prepreg and manufacture of printed wiring board |
| JP2001039034A (en) * | 1999-08-03 | 2001-02-13 | Mitsui Chemicals Inc | Optical recording medium |
| WO2002051821A1 (en) * | 2000-12-22 | 2002-07-04 | Astrazeneca Ab | Therapeutic compounds |
| AU2002365892A1 (en) * | 2001-11-30 | 2003-06-17 | Merck & Co., Inc. | Metabotropic glutamate receptor-5 modulators |
| UA83620C2 (en) * | 2001-12-05 | 2008-08-11 | Уайт | Substituted benzoxazoles and analogues as estrogenic agents |
| JP2003213086A (en) * | 2002-01-28 | 2003-07-30 | Sumitomo Bakelite Co Ltd | Resin paste for semiconductor and semiconductor device |
| WO2004003103A1 (en) * | 2002-07-01 | 2004-01-08 | Merck Patent Gmbh | Polymerizable, luminescent compounds and mixtures, luminescent polymer materials and their use |
| WO2004044062A1 (en) * | 2002-11-13 | 2004-05-27 | Asahi Glass Company, Limited | Actinic radiation curable coating composition and molded articles having coating films made from the composition through curing |
| JP2004210932A (en) * | 2002-12-27 | 2004-07-29 | Daicel Chem Ind Ltd | Curable resin composition and cured material |
| EP1593675A4 (en) * | 2003-02-14 | 2008-03-19 | Idemitsu Kosan Co | Hetero-polycyclic compounds, and coloring matters, pigments, dyes, color-changing material compositions, and color-changing films, made by using the compounds |
| JP4428505B2 (en) | 2003-07-09 | 2010-03-10 | 日本化薬株式会社 | Aromatic polyamide resin, epoxy resin composition and cured product thereof |
| ATE492581T1 (en) * | 2006-02-10 | 2011-01-15 | Basf Se | NEW POLYMERS |
-
2006
- 2006-03-28 JP JP2006087843A patent/JP4986485B2/en not_active Expired - Fee Related
-
2007
- 2007-03-14 US US12/280,418 patent/US7763700B2/en not_active Expired - Fee Related
- 2007-03-14 CN CN2011100766676A patent/CN102190777B/en not_active Expired - Fee Related
- 2007-03-14 WO PCT/JP2007/055106 patent/WO2007111136A1/en active Application Filing
- 2007-03-14 CN CN2007800064020A patent/CN101389684B/en not_active Expired - Fee Related
- 2007-03-22 TW TW096109827A patent/TWI403530B/en not_active IP Right Cessation
-
2008
- 2008-08-21 KR KR1020087020443A patent/KR101344704B1/en active IP Right Grant
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2004010996A1 (en) * | 2002-07-29 | 2004-02-05 | Shizuoka Coffein Co., Ltd. | 1,3-azole derivative and medicinal composition containing the derivative for treatment for thombosis |
| CN1747943A (en) * | 2003-02-14 | 2006-03-15 | 出光兴产株式会社 | Heteropolycyclic compound, and coloring matter, pigment, dye, color-changing material composition and color-changing film prepared therefrom |
| WO2005059001A1 (en) * | 2003-12-16 | 2005-06-30 | Toyo Boseki Kabushiki Kaisha | Curable composition |
Non-Patent Citations (1)
| Title |
|---|
| JP特开2001-39034A 2001.02.13 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN101389684A (en) | 2009-03-18 |
| CN102190777B (en) | 2012-09-05 |
| KR20080105044A (en) | 2008-12-03 |
| JP2007262204A (en) | 2007-10-11 |
| WO2007111136A1 (en) | 2007-10-04 |
| TWI403530B (en) | 2013-08-01 |
| JP4986485B2 (en) | 2012-07-25 |
| KR101344704B1 (en) | 2013-12-26 |
| CN102190777A (en) | 2011-09-21 |
| TW200804450A (en) | 2008-01-16 |
| US7763700B2 (en) | 2010-07-27 |
| US20090253887A1 (en) | 2009-10-08 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101389684B (en) | Curable epoxy resin composition | |
| CN106750226B (en) | The preparation method of phosphorous-containing polyester compound composition and phosphorus-containing flame-retardant epoxy resin solidfied material | |
| TWI396716B (en) | Epoxy resin composition, cured article, novel epoxy resin, novel phenol resin and semiconductor encapsulating material | |
| KR101143131B1 (en) | Epoxy compound, preparation method thereof, and use thereof | |
| JP5273762B2 (en) | Epoxy resin, epoxy resin composition and cured product thereof | |
| TWI400292B (en) | Used in glass fiber laminates high glass transition temperature resin varnish composition | |
| CN110520433A (en) | Phosphorous phenolic compounds, phosphorous epoxy resin, its hardening resin composition or composition epoxy resin and its solidfied material | |
| US4529790A (en) | Epoxy resin composition | |
| CN107083027A (en) | Oxazines resin combination and its manufacture method, prepreg, plywood and hardening thing | |
| TWI608048B (en) | Modified phenol resin, fabricating method of modified phenol resin, modified epoxy resin, fabricating method of modified epoxy resin, curable resin composition, cured object thereof and print circuit board | |
| KR20140129227A (en) | Polyvalent hydroxy resin, epoxy resin, method for producing same, epoxy resin composition and cured product thereof | |
| JP5233858B2 (en) | Epoxy resin composition, cured product thereof, and semiconductor device | |
| JP2008195843A (en) | Phenolic resin, epoxy resin, epoxy resin composition, and cured product of the same | |
| JP2012031281A (en) | Curable resin composition, cured product thereof, phenol resin, epoxy resin and semiconductor sealing material | |
| JP2000103941A (en) | Epoxy resin composition and semiconductor sealing material | |
| JP7477261B2 (en) | Hydroxy compound, its production method, resin composition and cured product thereof | |
| JP5435641B2 (en) | Phenol resin, epoxy resin, epoxy resin composition, and cured product thereof | |
| JP2001114863A (en) | Epoxy resin composition and its cured material | |
| JP4748695B2 (en) | Epoxy resin composition and cured product thereof | |
| JPH111546A (en) | Epoxy resin composition and electronic component | |
| JPS6377915A (en) | Phenol novolaks and its production | |
| JPS6215221A (en) | Epoxy resin composition | |
| JP4086630B2 (en) | Polyhydric phenol compound, epoxy resin composition and cured product thereof | |
| JP3118494B2 (en) | Curing agent for epoxy resin and epoxy resin composition | |
| JPH11181051A (en) | Epoxy resin composition, semiconductor-sealing material and resin-sealing type semiconductor-sealing machine |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20120530 Termination date: 20180314 |